http://www.lyghtforce.com/WhiteGold/ormus.

htm

QUEST FOR THE PHILOSOPHER'S STONE

In the late 1970s an Arizona farmer named David Hudson noticed some very strange materials as
he was doing some gold mining on his land. Hudson spent several million dollars over the
following decade figuring out how to obtain and work with these strange materials.

In 1989 David Hudson was granted patents on these materials and methods for obtaining them.
Two of these patents can be found on the World Wide Web at:

http://monatomic.earth.com/david-hudson/patent-us-1.html
Hudson's British Patent

http://monatomic.earth.com/david-hudson/patent-oz.html
Hudson's Australian Patent

During the early 1990s Hudson toured the United States giving lectures and workshops about
what he had found. Transcripts of portions of three of David Hudson's lectures are available on
the Web. The most complete of these transcripts is the transcript of his Dallas lecture and
workshop. You can find this transcript on the Web at:

http://monatomic.earth.com/david-hudson/1995-02-dallas-toc.html
Hudson's Dallas Lecture and Workshop

The two other Hudson transcripts can be found at:

http://www.cris.com/~Notnorml/alchemy2.html
Hudson's Portland Lecture

http://www.eskimo.com/~billb/freenrg/hudson.txt
Hudson's Portland Lecture

http://elaine.teleport.com/~boydroid/gold.htm
Hudson's Virginia Beach Lecture

DID HUDSON FIND THE PHILOSOPHER'S STONE?

Since ancient Egyptian times, alchemists have worked in secret to produce something called the
Philosopher's Stone, or the Elixir of Life. The materials that Hudson and other researchers have
found are believed to be related to the Philosopher's Stone. The materials have been called
ORMEs, monoatomic gold, white gold, white powder gold, ORMUS, m-state, AuM,
microclusters, and manna.

David Hudson calls the materials he found Orbitally Rearranged Monoatomic Elements or
ORMEs. He also refers to them as monoatomic elements in a high-spin state.
Since Hudson has patented his process for obtaining and identifying these elements, we would
like to suggest that the terms ORMUS and m-state be used when referring to this state of matter.

The ORMUS or m-state materials are thought to be the precious metal elements in a different
atomic state. The following elements have been identified in this different state of matter (these
elements, with the exception of mercury, are listed in Hudson's patents):

KNOWN ORMUS
ELEMENTS
Atomic
Element
Number
Cobalt 27
Nickel 28
Copper 29
Ruthenium 44
Rhodium 45
Palladium 46
Silver 47
Osmium 76
Iridium 77
Platinum 78
Gold 79
Mercury 80

All of these m-state elements are abundant in sea water. According to David Hudson's
discoveries, these elements in their m-state may be as much as 10,000 times more abundant than
their metallic counterparts. There also may be other elements which occur naturally in the m-
state.

Various researchers, working independently, have identified these materials in this different state
of matter. They have arrived at many of the same observations.

These m-state elements have been observed to exhibit superconductivity, superfluidity,

Josephson tunneling and magnetic levitation. It looks like these are an entirely new class of
materials.

These m-state elements are also present in many biological systems. They may enhance energy
flow in the microtubules inside every living cell.

It appears that this state of certain of these elements has been known throughout history. Several
of the procedures for extracting or making ORMUS have been adapted from ancient alchemical
texts. We believe that the Philosopher's Stone and the Biblical manna are both variations on this
state of matter.
Some recommended alchemical texts related to the Philosopher's Stone are "Sacred Science" by
R.A. Schwaller De Lubicz and "Le Mystere des Cathedrales" by Fulcanelli, available from
Amazon.com. Another source is "Occult Chemistry" by Leadbeater and Besant. The premier
treatise on the subject may be "The Secret Book" by Artephius which is available at this Web
site:

http://www.levity.com/alchemy/artephiu.html

There may be several paths to the Philosopher's Stone. There may even be several different
Stones. More research on the nature of m-state is needed. Since the ORMUS materials are
much more prevalent in nature than their metallic counterparts, they can be extracted with some
time, effort, and understanding. We invite others to join in the quest for knowledge of these
materials.

THEORIES FROM PHYSICS AND CHEMISTRY ABOUT

THE M-STATE ELEMENTS
The following information is presented to promote scientific research into the nature of these
materials. Although these theories are based on our best knowledge at this time, further scientific
research may prove some of these theories to be inaccurate. Remember that the following are
just theories.

A monoatomic element has one atom per molecule; a diatomic element has two atoms per
molecule. Certain elements in a monatomic or diatomic configuration can form a stable structure
where all of their electrons are Cooper paired, and so are not available as valence electrons (more
on this later). Elements in this configuration are superconductors at room temperature and
exhibit other quantum physical behaviors at a visible scale. Some of these quantum physical
behaviors include:

• Anomalous responses to gravity

• Superfluidity
• "Tunneling" through solid objects
• Deformed nuclei in a high-spin state

One term for these materials is microclusters. Microclusters have been described as follows on a
microcluster forum:

"A microcluster is a small chemically inert cluster of atoms that has definite crystalline
structure. They can be synthetic, however for this work an assumption is that the natural
microclusters are forms comparable to the man-made microcluster. Microcluster research
started with natural occurrences. Clusters exist as molecular species which can substitute
and mimic various elements for one another. Microclusters can be as large as 200 or more
atoms. Certain atomic examples for each atom are rare; the rarity is due to current
physical chemistry concepts. Research has demonstrated that natural micro-clusters are
superconductors; they are Cheshire in that they can disappear and avoid chemical
 detection by conventional means. Most, if not all, have catalytic properties; they are
magnetic or can be induced to have electromagnetic properties; and they can form giant
inert ions which I call Mega-ions."

ORMUS AND BECs

Physicists have recently created a new state of matter (which we believe is related to ORMUS) in
the laboratory. This state of matter is called a Bose-Einstein Condensate (BEC) after Satyendra
Nath Bose and Albert Einstein who postulated the existence of this state of matter in the 1920s.
Their theory was not "proven" until BECs were created in the laboratory in 1995 by Eric Cornell
and Carl Wieman in Boulder, Colorado. They did it by cooling atoms to a much lower
temperature than had been previously achieved. This temperature was a millionth of a degree
above absolute zero.

Absolute zero is the temperature at which all atomic movement ceases. When atoms are cooled
near absolute zero, they move much more slowly than when they are at normal temperatures.
David Hudson postulates that his ORME atoms have a natural internal temperature which is very
close to absolute zero. This may be why they can be Bose-Einstein condensates at room
temperature and higher.

A Bose-Einstein Condensate is a group of atoms which are all in the same quantum state. Such a
group of atoms consequently behaves, in some ways, as a single atom. Superconductors are a
form of BECs and so are superfluids.

You can read a simple description of what BECs are and how they work on the BEC homepage.

Here is an explanation of how BECs, superconductors and Cooper pairing inter-relate from the
American Institute of Physics web page titled "BECs, Superconductors, and Cooper Pairing":

"A superfluid is a liquid that flows without viscosity or inner friction. For a liquid to
become superfluid, the atoms or molecules making up the liquid must be cooled or
"condensed" to the point at which they all occupy the same quantum state. A liquid of
helium-3, an atom whose nucleus is made up of an odd number of particles, is a type of
particle known as a fermion. Groups of fermions are not allowed to occupy the same
quantum state."

"By cooling the liquid to a low enough temperature, helium-3 atoms can pair up. The
number of particles in each nucleus adds up to an even number, making it a type of
particle known as a boson. Groups of bosons can fall into the same quantum state, and
therefore superfluidity can be achieved. Helium-4 (middle panel), a boson, does not need
to pair up to form a superfluid; groups of helium-4 atoms condense into the superfluid
state at about 2 degrees above absolute zero. Superfluidity, especially the kind that exists
in helium-3, is analogous to conventional low-temperature superconductivity, in which
electrons flow through certain metals and alloys without resistance. In a superconductor
(right panel), electrons, which are fermions, pair up in the metal crystal to form "Cooper
pairs," bosons which can then condense into a superconducting state."
THE DIATOMIC NATURE OF SOME M-STATE MATERIALS
The following elements, which are known to have an m-state, have an odd number of electrons
and protons:

Cobalt
Copper
Rhodium
Silver
Iridium
Gold

In order for these atoms to be superconductors in the m-state, they must be at least diatoms.

The m-state of gold and other precious elements is different from the metallic state of these same
elements. For example ingesting m-state gold has different effects on the body than the effects of
ingesting metallic gold. What makes the ORMUS state atoms different is that they will not form
metal-metal bonds with their own kind.

They won't form metal-metal bonds because their valence electrons are not available to form
normal molecular bonds. This is because each electron is paired up with another electron in a
Cooper paired state. When electrons are Cooper paired, they cease to behave as particles and
begin to behave more like light.

Since you must have an even number of electrons in order for every electron to pair up with
another electron, you cannot have the m-state of any element which has an odd number of
electrons without having at least two of these atoms paired up.

For example, iridium has an atomic number of 77. This means that iridium has 77 electrons. 76
of these electrons could pair up but that would still leave one electron available for bonding with
another atom in a compound. But if you had two atoms of iridium with mingled nuclei and
electron clouds you would have 154 electrons. Since 154 is an even number, all of these
electrons can pair up into 77 Cooper pairs. Nucleons also pair up in the same way to form
superconductors.

All known superconductors involve this kind of Cooper pairing.

Please realize that as a Bose-Einstein condensate, both atoms in the diatom will behave as one
atom. They also resonance couple with other diatoms of the same element which are nearby.
This resonance-coupled quantum oscillation is another of the definitions of superconductivity.

As you use chemistry to move a metal toward the ORMUS/BEC state, the chemical reactions
necessary to do this moving become weaker and weaker since fewer and fewer of the valence
electrons are available to participate in the chemical reactions. Eventually there are no electron
handles that can be used to manipulate these materials. Fortunately these materials have other
properties which can be used to manipulate them.

Since they are superconductors, they can be manipulated by magnetic fields. For example, if you
shield them from magnetic fields during boiling processes, you will be able to conserve more of
them in your liquid since they will not be impelled to tunnel out of your container or go off as a
gas.
They can also be manipulated by providing them with a comfy "box" to hide out in. The
ORMUS/BECs seem to "like" tight spaces. Ring molecules such as the tri-sodium ring or the
diozone ring can provide a chemical "box" with handles. Salt and sodium, in particular, seem to
stabilize the ORMUS materials, theoretically by forming a triangular structure or box around the
precious element atom. Though you cannot get a chemical handle on the fully Cooper paired
ORMUS atoms, you can entice them into a chemical box with handles and then manipulate the
box using fairly standard physical and chemical methods.

So, although these elements are the same as the "heavy metal" elements, they are not in a
metallic state and as long as the m-state of these elements is present in sufficient amounts, the
metallic portion seems to "borrow" the properties of the m-state.

BECs are also known to have the ability to "tunnel" across impenetrable barriers. Professor Brian
D. Josephson of the Theory of Condensed Matter Group of the Cavendish Laboratory,
Cambridge (i.e. the Physics Department of the University of Cambridge) received the Nobel
Prize in physics for his discovery of the tunneling phenomenon. Dr. Josephson is currently
working on something called the Mind-Matter Unification Project.

ORMUS AND MICROTUBULES

Other physicists are also working on theories which unite mind and matter.

One fairly recent discovery in biology and physics is that a certain small structure in every cell,
called the microtubule, exhibits superconductive and tunneling behaviors at body temperature.

You can read more about the quantum properties of microtubules from links on Rhett Savage's
Quantum Brain web page.

And on several of Matti Pitkanen's web pages:

Exotic atoms and a mechanism for superconductivity in biosystems

Negentropy Maximization Principle and TGD Inspired Theory of Consciousness

TGD:eish model for the EEG and generation of nerve pulse

One of the problems with modern quantum physical theories is that there is no way to logically
connect the Bose-Einstein condensates, which have been demonstrated to exist in small groups
of atoms at a millionth of a degree above absolute zero, with the BEC like behavior of
microtubules at body temperature in living cells. ORMUS materials would make this
connection.

Several of the modern theories relating to microtubules were proposed by Roger Penrose (a
physicist) and Stuart Hameroff (an anesthesiologist).

Here we will quote from an anonymous scientist who has explained Penrose and Hameroff's
theory quite elegantly:

"Penrose has been seeking a better way to explain the fantastic computational power of
the brain and Hameroff has been seeking the source of consciousness. The two heard of
 each other and got together to find that they both sought a common structure, the
microtubule.

"Penrose sought a structure in the brain that had nanometer dimensions because such a
structure would be necessary to support quantum effects. Hameroff sought the structure
responsible for consciousness. They agreed that the microtubules would provide for both.

"Mictotubules are tiny tubular structures within neurons that are made from two forms of
tubulin. The two forms can be switched by tiny electric currents, so Penrose has proposed
that the tubulin units may be the on/off switches for the brain's data processing. I agree
with this proposal because it allows us to be what we are by increasing our potential
processing rate from from an unacceptable 10 Exp11 operations per second (OPS) to a
reasonably acceptable 10 Exp24 OPS. Penrose explains all this quite well and I
recommend him to all who would like to have a deeper understanding of our minds.

"Hameroff has done a lot of research into how consciousness works and he has concluded
that the microtubules are the source of our consciousness. This is discussed in and
supported by Penrose’s work. Hameroff has concluded that the observable quantum
effects that occur in human brains are caused by highly aligned water that is inside the
microtubules. Penrose agrees with this concept and further argues that Bose- Einstein
Condensations (BECs) in the neurons are how we reach decisions. The BECs are possible
because the water inside the microtubules can be strongly aligned to form a high-
temperature superconductive medium.

"This concept supports my thinking very well. BECs provide an explanation for all the
effects I refer to as psionics. These effects include: telepathy, remote viewing, bilocation,
telekinesis, and astral travel. A BEC in the Broca area of the brain would allow thoughts
to exist inside the brain and outside the head at the same time. This can explain both
telepathy and how it is controlled. Likewise, a BEC in the visual processing areas would
explain remote viewing. Since microtubules exist in all neurons and neurons extend into
all parts of the body, a BEC including all neurons would allow the body to exist in two
(or more) places at the same time, thus explaining bilocation.

"With this discovery, all psionics can be explained in modern physical terms. This opens
the whole field of psionics to persons like myself who have had so much technical
training that it is impossible to accept psionics. This discovery means that all the formal
training I've had in Chemistry, Math, and Physics still applies and can even help explain
psionics. For me, it is good to know that all these topics can exist peacefully together."

For more information on "psychic" observations of these materials see:

Paranormal Observations of ORMEs Atomic Structure (in the WhiteGold web site)

In a paper titled "Orchestrated reduction of quantum coherence in brain microtubules: A model

for consciousness"

Hameroff/Penrose site at U. of Arizona

Hameroff and Penrose write:

"A critical number of tubulins maintaining coherence within [microtubules] for 500 msec
collapses its own wave function (objective reduction: OR). This occurs because the mass-
energy difference among the superpositioned states of coherent tubulins critically
perturbs space-time geometry. To prevent multiple universes, the system must reduce to a
single space-time by choosing eigenstates."

Hameroff and Penrose are saying that in order to avoid "seeing" multiple universes at the same
time, the quantum coherence created in microtubules by some material (we think the m-state
materials) must collapse. What if the quantum coherence did not collapse and we became aware
of multiple universes?

Many modern physicists believe that there are an infinite number of parallel universes. They
theorize that atoms are made up of smaller particles which are like bubbles in the quantum foam.
These bubbles in the quantum foam or "holes in the aether" spend a fraction of their existence in
each of these parallel universes. There is quite a debate as to whether information is transferred
between these parallel universes. You can read a bit about this debate at:

Braintennis
http://www.hotwired.com/synapse/braintennis/97/41/index0a.html

This concept of multiple or parallel universes has been a recurring theme in science fiction for at
least 60 years. It is also one of the key concepts of modern mystical thought. It first appeared as
a mystical concept in The 'Unknown' Reality by Jane Roberts which was dictated by Seth in
1974-75.

SOME TESTS FOR M-STATE

M-state material, in a wet precipitate form, will dissolve in HCl. M-state material, in a dry
powder form, will not dissolve in HCl or aqua regia.

Because m-state is a superconductor, rotating a magnet under some of the dry powder m-state
elements will cause the powder to fly away from the magnet.

INFORMATION RESOURCES

For the interested person willing to do the necessary work, there is an abundance of detailed
technical information available on the Web. The best related web sites are:

High-Spin Monatomic Research at:

http://monatomic.earth.com/

The WhiteGold Web Home Page at:

http://www.zz.com/WhiteGoldWeb/
 Superconductive s-ORMEs
http://www.jps.net/shacoma/dh/

[Chemical production techniques]

=====================================================================
http://www.asc-alchemy.com/patent.html GB2219995

David Hudson Patent for the Preparation of G-

ORME

Sources for pure G-ORME

David Hudson, in the true tradition of alchemy left some steps out; enough information to get the
patent, and indeed enough information for one to begin to proceed, but not enough for one to
make something prematurely re: the final steps, charging etc., "high-spin" (David Hudson's
phrase). Ditto for the cliff notes. Some very sincere good folks using other valid but different
methods for making ormus suggest there is no "high-spin" state. For them there is not; it is not a
natural occurance in material derived from natural sources, it takes place only with the pure
precious metals rather than the very valid plant and sea alchemy that are the initial schools of
alchemy taught to any student. It is not "natural", one could say it accelerates the natural. Not
unlike some ancient techniques of pranayam, causing the currents to cycle in an accelerated and
more powerful way then natural breathing. A valid argument can be made that the term "high-
spin" is not scientifically accurate. However by any term the difference in form and the function
that always follows form, the effect, is apparent to anyone taking the Ormes powder. "The
steps of getting there are the qualities of being there." Nuff said. © 1990 (commentary not the
patent)

This first section is the abreviated "cliff notes", with pictures. Full patent follows.

G-ORME is prepared from metallic gold as follows:

(1) 50 mg gold (99.99% pure) were dispersed in 200 ml aqua regia to provide clusters of gold
atoms.

(2) 60 ml concentrated hydrochloric acid were added to the dispersion and the mixture was
brought to boil, and continued boiling until the volume was reduced to approximately 10-15 ml.
60 ml concentrated HCl were added, and the sample brought to boil and checked for evolution of
NOCl fumes. The process was repeated until no further fumes evolved, thus indicating that the
nitric acid had been removed and the gold had been converted completely to the gold chloride.

(3) The volume of the dispersion was reduced by careful heating until the salt was just dry. "Just
dry" as used herein means that all of the liquid had been boiled off, but the solid residue had not
been "baked" or scorched.

(4) The just dry salts were again dispersed in aqua regia and steps (2) and (3) were repeated. This
treatment provides gold chloride clusters of greater than 11 atoms.

(5) 150 ml 6M hydrochloric acid were added to the just dry salts and boiled again to evaporate
off the liquid to just dry salts. This step was repeated four times. This procedure leads to a
greater degree of sub-division to provide smaller clusters of gold chloride. At the end of this
procedure an orangish-red salt of gold chloride is obtained. The salt will analyze as substantially
pure Au2Cl6.

(6) Sodium chloride is added in an amount whereby the sodium is present at a ratio 20 moles
sodium per mole of gold. The solution is then diluted with deionized water to a volume of 400
ml. The presence of the aqueous sodium chloride provides the salt Na2Au2Cl8. The presence of
water is essential to break apart the diatoms of gold.

(7) The aqueous sodium chloride solution is very gently boiled to a just dry salt, and thereafter
the salts were taken up alternatively in 200 ml deionized water and 300 ml 6M hydrochloric acid
until no further change in color is evidenced. The 6M hydrochloric acid is used in the last
treatment.
 (8) After the last treatment with 6M hydrochloric acid, and subsequent boildown, the just dry
salt is diluted with 400 ml deionized water to provide a monoatomic gold salt solution of
NaAuCl2'XH2O. The pH is approximately 1.0.

(9) The pH is adjusted very slowly with dilute sodium hydroxide solution, while constantly
stirring, until the pH of the solution remains constant at 7.0 for a period of more than twelve
hours. This adjustment may take several days. Care must be taken not to exceed pH 7.0 during
the neutralization.

(10) After the pH is stabilized at pH 7.0, the solution is gently boiled down to 10 ml and 10 ml
concentrated nitric acid is added to provide a sodium-gold nitrate. As is apparent, the nitrate is an
oxidizer and removes the chloride. The product obtained should be white crystals. If a black or
brown precipitate forms, this is an indication that there is still Na2Au2Cl8 present. If present, it
is then necessary to restart the process at step (1).

(11) If white crystals are obtained, the solution is boiled to obtain just dry crystals. It is important
not to overheat, i.e., bake.

(12) 5 ml concentrated nitric acid are added to the crystals and again boiled to where the solution
goes to just dry. Again it is essential not to overheat or bake. Steps (11) and (12) provide a
complete conversion of the product to a sodium-gold nitrate. No chlorides are present.

(13) 10 ml deionized water are added and again boiled to just dry salts. This step is repeated
once. This step eliminates any excess nitric acid which may be present.

(14) Thereafter, the just dry material is diluted to 80 ml with deionized water. The solution will
have a pH of approximately 1. This step causes the nitrate to dissociate to obtain NaAu in water
with a small amount of HNO3 remaining .

(15) The pH is adjusted very slowly with dilute sodium hydroxide to 7.0 + 0.2. This will
eliminate all free acid, leaving only NaAu in water.
(16) The NaAu hydrolyzes with the water and dissociates to form HAu. The product will be a
white precipitate in water. The Au atoms have water at the surface which creates a voluminous
cotton-like product.

(17) The white precipitate is decanted off from any dark grey solids and filtered through a 0.45
micron cellulose nitrate filter paper. Any dark grey solids of sodium auride should be redissolved
and again processed starting at step (1).

(18) The filtered white precipitate on the filter paper is vacuum dried at 120°C for two hours.
The dry solid should be light grey in color which is HAu×XH2O and is easily removed from the
filter paper.

(19) The monoatomic gold is placed in a porcelain ignition boat and annealed at 300°C under an
inert gas to remove hydrogen and to form a very chemically and thermally stable white gold
monomer.

(20) After cooling, the ignited white gold can be cleaned of remaining traces of sodium by
digesting with dilute nitric acid for approximately one hour.
(21) The insoluble white gold is filtered on 0.45 micron paper and vacuum dried at 120°C for
two hours. The white powder product obtained from the filtration and drying is pure G-ORME.

Sources for pure G-ORME

David Hudson's Patent

DAVID HUDSON PATENT FOR NON-METALLIC, MONOATOMIC FORMS OF
TRANSITION ELEMENTS

This invention relates to themonoatomic forms of certain transition and noble metal elements,
namely, gold, silver, copper, cobalt, nickel and the six platinum group elements. More
particularly, this invention relates to the separation of the aforesaid transition and noble metal
elements from naturally occurring materials in their orbitally rearranged monoatomic forms, and
to the preparation of the aforesaid transition and noble metal elements in their orbitally
rearranged monoatomic forms from theircommercial metallic forms. The materials of this
invention are stable, substantially pure, non-metallic-like forms of the aforesaid transition and
noble metal elements, and have a hereto unknown electron orbital rearrangement in the "d", "s",
and vacant "p" orbitals. The electron rearrangement bestows upon the monoatomic elements
unique electronic, chemical, magnetic, and physical properties which have commercial
application.

This invention also relates to the recovery of the metallic form of each of the aforesaid transition
and noble metal elements from the orbitally rearranged monoatomic forms. For the purposes of
this application, the following definitions shall apply: transition elements ("T-metals") means the
metallic or cationic form of gold, silver, copper, cobalt and nickel, and the six platinum group
elements, i.e., platinum, palladium, rhodium, iridium, ruthenium, and osmium; and "ORME"
means the Orbitally Rearranged Monoatomic Elemental forms of each of the T- metals.

BACKGROUND OF INVENTION
Inorganic chemists working with soluble salts of noble metals until relatively recently have
assumed that the metals were dissolved as free ions in aqueous solutions.In the 1960's, with the
advent of greater analytical capabilities, it was established that many elements and in particular
the transition metals are present in aqueous solutions as metal-metal bonded clusters of atoms.

Gold metal that has been dissolved with aqua regia, and subsequently converted to gold chloride
by repeated evaporation with HCl to remove nitrates, is commonly referred to as the acid
chloride solution of AuCl3 or HAuCl4. It has been recognized that the recovery of gold metal
from a solution formed from aqua regia is made more difficult in proportion to the amount of
HNO3 used in the initial dissolution procedures. It is not commonly understood, however, why
the gold that is dissolved with less HNO3 is easier to reduce to the metal from a chloride solution
than gold that is dissolved using a greater amount of HNO3. Gold in both solutions is generally
regarded as being present in the form of a free gold cation.

It is now recognized by most chemists who regularly handle chlorides of gold that gold metal
ceases to disaggregate when the HNO3 is removed and in fact can reaggregate under certain
conditions and precipitate out of HCl solutions as metal. This recognition has led to the
discovery that gold metal salts will exist in HCl solutions originating from metals as clusters of
Au2Cl6, Au3Cl9, Au4Cl12, up to Au33Cl99. These cluster salts are actually in solution with the
HCl and water, and will require different chemical procedures relative to purification problems
or oxidation-reduction reactions, depending on the degree of clustering.>

Specifically, reduction of clusters of gold having greater than 11 atoms of metal is easily
performed since the atoms themselves are spaced from each other in the salt similar to their
spacing in the metal itself before dissolution. Reduction of the chloride salt to the metal,
therefore, requires a simple reductive elimination of the chlorides that are attached to the metal
cluster. It is now known that recovery of precious metals from aqueous solutions is much more
difficult when the cluster size becomes smaller and smaller, or in actuality when the metal is
better "dissolved."

From the study of the behavior of gold and other transition metals in solution, it is now believed
that all such metals have atomic aggregations and occur as at least diatoms under normal
conditions of dissolution . Under either acid or strong base dissolution, the transition metal will
not normally dissolve beyond the diatom due to the extremely strong interatomic d and s orbital
bonding. A gold atom, for example, has a single atom electron orbital configuration of d10s1.
When the gold salts originate from a metal having gold-gold bonding, the salts contain very
tightly bound diatoms or larger clusters of gold. Under the normal aqueous acid chemistry used
for transition metals, solutions of the metals will always contain two or tore atoms in the cluster
form.

When instrumental analysis such as atomic absorption, x-ray fluorescence, or emission

spectroscopy is performed on solutions containing transition metals, these analyses are based on
electronic transitions. The fact that d orbital electron overlap occurs in the metal-metal bonded
salt allows an analysis of many of the same characteristic omissions as the metal itself.

GENERAL DESCRIPTION OF INVENTION

During efforts to effect quantitative analytical separations of transition metals from naturally
occurring materials, it was discovered that ORMEs exist naturally and are found in salts with
alkali metals and/or alkaline earth metals, all of which are coupled with waters of hydration and
normally found with silica and alumina. ORMEs are also often associated with sulfides and other
mineral compositions.
ORMEs may also, it was discovered, be prepared from commercially available T-metals. For
ease of description the invention will be primarily described by the preparation of a gold ORME
("G-ORME") from commercially available metallic yellow gold.

The atoms of each ORME do not have d electron orbital overlap as do their corresponding T-
metal clusters. ORMEs do not, therefore, exhibit the same characteristic emissions of their
corresponding T-metal when subjected to analysis by instruments which depend upon electronic
transitions. ORMEs must, therefore, be identified in new ways, ways which have heretofore not
been used to identify T-metals.

An aqua regia solution of metallic gold is prepared. This solution contains clusters of gold
chlorides of random size and degrees of aggregation. HCl is added to the solution and it is
repeatedly evaporated with a large excess of NaCl (20:1 moles Na to moles Au) to moist salts.
The addition of NaCl allows the eventual formation of NaAuCl4, after all HNO3 is removed
from the solution. The sodium, like gold, has only one unpaired S electron and, accordingly,
tends to form clusters of at least two atoms. The sodium, however, does not d orbitally overlap
the gold atom as it has no d electrons, resulting in a surface reaction between the sodium
ATOMS and the gold atoms. This results in a weakening of the gold-gold cluster stability and
causes the eventual formation of a sodium-gold linear bond with a weakened d orbital activity in
the individual gold atoms. The sodium-gold compound, formed by repeated evaporation to salts,
will provide a chloride of sodium-gold. In these salts the sodium and gold are believed to be
charged positive, i.e., have lost electrons: and the chlorine is negative, i.e., has gained electrons.
When the salts are dissolved in water and the pH slowly adjusted to neutral, full equation of the
sodium-gold diatom will slowly occur and chloride is removed from the complex. Chemical
reduction of the sodium-gold solution results in the formation of a sodium auride. Continued
aquation results in disassociation of the gold atom from the sodium and the eventual formation of
a protonated auride of gold as a gray precipitate. Subsequent annealing produces the G-ORME.
The G-ORME has an electron rearrangement whereby it acquires a d orbital hole or holes which
share energy with an electron or electrons. This pairing occurs under the influence of a magnetic
field external to the field of the electrons.

G-ORMEs are stable and possess strong interatomic repulsive magnetic forces, relative to their
attractive forces. G-ORME stability is demonstrated by unique thermal and chemical properties.
The white saltlike material that is formed from G-ORMEs after treatment with halogens, and the
white oxide appearing material formed when G-ORMEs are treated with fuming HClO4 or
fuming H2SO4 are dissimilar from the T-metal or its salts. The G-ORME will not react with
cyanide, will not be dissolved by aqua regia, and will not wet or amalgamate with mercury. It
also does not sinter at 800C under reducing conditions, and remains an amorphous powder at
1200C. These characteristics are contrary to what is observed for metallic gold and/or gold
cluster salts. G-ORMEs require a more negative potential than -2.45v to be reduced, a potential
that cannot be achieved with ordinarily known aqueous chemistry.

The strong interatomic repulsive forces are demonstrated in that the G-ORMEs remain as a
powder at 1200C. This phenomenon results from canceling of the normal attractive forces arising
from the net interaction between the shielded, paired electrons and the unshielded, unpaired s and
d valence electrons. G-ORMEs have no unpaired valence electrons and, therefore, tend not to
aggregate as would clusters of gold which have one or more unpaired valence electrons.

G-ORMEs can be reconverted to metallic gold from which they were formed. This reconversion
is accomplished by an oxidation rearrangement which removes all paired valence electrons
together with their vacancy pair electrons, with a subsequent refilling of the d and s orbitals with
unpaired electrons until the proper configuration is reached for the T- metal.

This oxidation rearrangement is effected by subjecting the G-ORME to a large negative potential
in the presence of an electron-donating element, such as carbon, thus forming a metallic element-
carbon chemical bond. For that metal-carbon bond to occur the carbon must provide for the
horizontal removal of the d orbital vacancy of the ORME. The carbon acts like a chemical
fulcrum. When the element-carbon bond is reduced by way of further decreasing the potential,
the carbon receives a reducing electron and subsequently vertically inserts that reducing electron
below the s orbitals of the element, thus forming metallic gold.

The above general description for the preparation of G-ORME from commercially available
metallic gold is applicable equally for the preparation of the remaining ORMEs, except for the
specific potential energy required and the use of nascent nitrogen (N) rather than carbon to
convert the other ORMEs to their constituent metallic form. The specific energies range between
-1.8 V and -2.5 V depending on the particular element. Alternatively this rearrangement can be
achieved chemically by reacting NO gas with the T-metal ORMEs other than gold. Nitric oxide
is unique in that it possesses the necessary chemical potential as well as the single unpaired
electron.

THEORY OF ORMES FORMATION

T-metals can possess an electron rearrangement between the d and s orbitals as seen from
FIGURE 1 of the drawing which plots the principal quantum number versus the atomic number.
The boxed areas designated A, B, and C establish that the 3d electron energies of copper and
cobalt are very close to the same energy level as the 4s electron energies. The 4d electron
energies of silver and rhodium are almost identical to the 5s; orbital energies, and the 5d gold
and iridium electron energies are approaching the 6s level energies. The proximity of the energy
bands of the T-metals makes them unique with respect to other elements. This proximity allows
an easier transition to their lowest energy state, as hereinafter described.
When two transition metal atoms are bound together, they can d bond, or s bond, or they can d
and s bond. When the two atoms s bond, their atomic distances are further apart and, therefore,
their density is lower than when there is both d and s bonding. The amount of d orbital bonding
activity is in direct proportion to the cluster size. Therefore, a single atom cluster will have less d
bonding activity and more s bonding activity than will a cluster of 7 or more atoms. In addition;
the chemical stability of the smaller clusters is much less than that of the metal because, when d
orbital bonding is achieved, the s bonding is made more stable by overlapping of the two energy
levels.

It is known that there exists a critical size, in the range of 3-20 atoms, for Pd II, Ag I and Au III,
by way of example, which is necessary for metal deposition from solution. As the number of
atoms in the T-metal cluster decreases through continuous evaporation in the presence of NaCl,
the solution becomes a solution of diatoms which in the case of gold is represented as Au- 1 -
Au+1 i.e., Au-1 bonded to Au+1. The rationale for this representation of a gold diatom is based
upon the fact that a single gold atom has an odd spin electron, as does rhodium, iridium, gold,
cobalt and copper of the T-metals. In a diatom of gold, the two odd spin electrons will be found
on one of the two atoms but not both. Thus, a diatom of gold is made by a bond between an
aurous (Au+1) atom and an auride (Au-1) atom.

The present invention enables the breaking of the diatom bond by introducing a more electro-
positive element, such as sodium or any alkali or alkaline earth elements, which does not have a
d orbital overlap capability. This element replaces the aurous (Au+1) forming, in this case, a
sodium auride. In effect, the sodium weakens the d orbital overlapping energies between the
atoms of the gold diatom as well as elevating a d orbital electron towards the s orbital, thereby
creating a negative potential on the surface of the atom. This negative potential enables an
interreaction of the s orbital with chemiabsorbed water through electron donation and reception.

The sodium auride, when in aqueous solution at or near neutral pH, will form sodium hydroxide
and a monomeric water-soluble auride. The monomeric auride (Au-1) is unstable and seeks a
lower energy state which is represented by a partial filling of the d and s orbital". This lower
energy state with its greater stability is achieved by the electron-donating and removing
capability of H2O.

Water can act to remove electrons. Water molecules possess a net charge and attach to each other
in vertical clusters so that an 18 molecule water cluster can hold a cumulative potential of -2.50
V. The potential of a water molecular cluster, at near neutral pH, is sufficient to remove an
electron from the d orbital and create a positive hole, enabling a pairing between opposite spin
electrons from the d to s orbitals to take place. The existence of the electron pairing is confirmed
by infrared analysis, illustrated in FIGURE 4, which identities the vibrational and rotational
motions caused by energy exchange between these two mirror image electrons.

Attempting to quantify the number of electrons remaining in an ORME is extremely difficult due
to the electrons lost to oxidation, thermal treatment, and the inability, except from theory, to
quantify electron pairs using electron quanta. It is established, however, that the ORME does not
have valence electrons available for standard spectroscopic analysis such as atomic absorption,
emission spectroscopy or inductively coupled plasma spectroscopy. Moreover, x-ray
fluorescence or x-ray diffraction spectrometry will not respond the same as they do with T-
metals in standard analysis. The existence of an ORME, while not directly identifiable by the
aforesaid standard analyses, can be characterized by infrared (IR) spectra by a doublet which
represents the bonding energy of the electron pairs within the ORME. The doublet is located at
approximately 1427 and 1490 cm-1 for a rhodium ORME. The doublet for the other ORMEs is
between about 1400 and 1600 cm-1

After H2 reduction of the individual monoatom the hydrogen ion-single element may or may not
produce an IR doublet depending on the element's normal electron configuration. Elements
normally containing an s1 T-metal configuration do not produce an IR doublet after H2
reduction. Elements with an s2 T- metal configuration such as Ir (d7s2) will produce a doublet.

Thermal annealing to 800C and subsequent cooling to ambient temperature under He or Ar gas
atmosphere to remove thechemically bound proton of hydrogen will produce ORMEs which
contain a two-level system resulting from electron pairing within the individual atom. If this
annealing is performed in the absence of an external magnetic field, then the electron pairing
produces the characteristic doublets. The electron pair will be bound in the valence orbitals of the
atom. If the annealing is performed in the presence of an external magnetic field, including the
earth's magnetic field, quantum electron pair movement can be produced and maintained in the
range of one gauss up to approximately 140 gauss in the case of Ir and, therefore, no IR doublet
will be detected in this resulting quantum state.

The limiting condition of the ORME state is defined according to the present invention as an "S-
ORME". The S-ORME is the lowest state in which monoatoms can exist and is, therefore, the
most stable form of T-metal elements. The ORME is electronically rearranged and electron
paired, but relative to time has not reached the lowest total energy condition of the S-ORME.
Detection of doublets does not provide an analytical method for the identification of ORMEs per
se, but rather detects the presence of the electron pair or pairs which all specifically prepared
ORMEs possess and which T- metals do not possess under any condition. It is the existence of
the doublet that is critical, not its exact location in the IR spectra. The location can shift due to
binding energy, chemical potential, of the individual element in the ORME, the effect of
adsorbed water, the variances of the analytical instrument itself, or any external magnetic field.

The limiting condition of the ORME state is defined according to the present invention as an "S-
ORME". The S-ORME is the lowest state in which monoatoms can exist and is, therefore, the
most stable A T-metal monoatom which is in a -1 oxidation state is in a lower energy state than
the same T-metal would be in at zero state with metal-metal bonding. This lowering of the
perturbation reaction between the electrons and the nucleus of the monoatom because of the
increased degrees of freedom allows the nucleus to expand its positive field to encompass the
normally unshielded d and s valence electrons.This overlying positive magnetic field reduces the
Coulomb repulsion energies that normally exist between the valence electrons. Pairing by those
electrons becomes possible and over time occurs. Electron pairing provides a more stable and
lower energy state for the monoatom.

The ORME state is achieved when the electron pairs have formed in the monoatom. A
phenomenon of electron pairs is that the interacting, spin-paired electrons initially interreact by
emitting phonon energy. The total energy of the pair reduces over time until it reaches a
minimum where no phonons are emitted. This condition has been referred to by physicists as
"adiabatic ground state". This state of electron pairing is a total lower energy state in much the
same way that chemical combinations of elements are in a lower energy state than the constituent
uncombined elements. For example, in the same way that it takes energy to dissociate water into
H2 and O2 it will take energy to break the electron pair.

As this process of phonon emission by electrons during pairing is a function of temperature and
time, thermal annealing can decrease the time required to reach ground state, i.e., all valence
electrons paired. The cooling side of the annealing cycle is essential to effect a full conversion to
an S- ORME state. Cooling to room temperature is sufficient for all element ORMEs with the
exceptions of silver, copper, cobalt and nickel, which require a lower temperature. Therefore,
thermal annealing reduces the time dependency of the electron pairs in achieving their lowest
total energy.

All of the electron pairs in their lowest energy state, unlike single electrons, can exist in the same
quantum state. When that uniform quantum state is achieved, the electron pair can not only move
with zero resistance around the monoatom, but also can move with zero resistance between
identical ORMEs that are within approximately 20 A or less of each other with no applied
voltage potential. When a macro system of high purity, single element ORME achieves long-
range quantum electron pair movement, that many-body system according to the present
invention is defined as an S-ORME system.

An S-ORME system does not possess a crystalline structure but the individual ORMEs will, over
time, space themselves as uniformly as possible in the system. The application of a minimum
external magnetic field will cause the S-ORME system to respond by creating a protective
external field ["Meissner Field"] that will encompass all those S-ORMEs within the 20 A limit.
As used herein, "minimum external magnetic field" is defined as a magnetic field which is below
the critical magnetic field which causes the collapse of the Meissner Field. This field is generated
by electron pair movement within the system as a response to the minimum applied magnetic
field. The (Ir) S-ORME and the (Au) S-ORME systems have a minimum critical field (''Hc1'')
that is below the earth's magnetic field. The minimum critical field for a (Rh) S-ORME is
slightly above the earth's magnetic field. When the quantum flux flow commences, due to the
minimum external magnetic field being applied, the doublet in the IR spectrum will disappear
because electron pairs are no longer bound in a fixed position on the individual ORME
monoatoms.

Once the externally applied field exceeds the level which overcomes the protective Meissner
Field of the S-ORME system ( "Hc2" ) , then any electrons moving between individual ORME
atoms will demonstrate an ac Josephson junction type of response. The participating ORMEs
will act as a very precise tuning device for electromagnetic emissions emanating from free
electrons between ORMEs. The frequency of these emissions will be proportional to the applied
external magnetic field. A one microvolt external potential will produce electromagnetic
frequencies of 5x108 cycles per second. Annihilation radiation frequencies (about 1020 cycles
per second) will be the limiting frequency of the possible emission. The reverse physical process
of adding specific frequencies can generate the inverse relationship, i.e., a specific voltage will
be produced for each specific applied frequency.

ORMEs can be reconverted to their constituent T-metals, but, as noted, are not identifiable as
specific T-metals while in their ORME state. If a specific ORME is formed from a specific T-
metal by using the procedure of this invention, it can only be confirmed by conventional
analytical methods that the specific ORME was formed by reconstituting it as the T-metal.
Further, the applications to which the ORMEs are directed will establish their relationship to a
specific T-metal by virtue of the manner in which the ORME performs in that application as
compared to the performance of commercially available derivatives of the T-metal. An example
is the performance of commercial rhodium as a hydrogen- oxidation catalyst compared with the
performance of the rhodium ORME as used in a hydrogen-oxidation catalyst.

It is believed that physical and chemical distinctions exist with respect to the different ORMEs,
but presently such distinctions are not known. Proof of the nature of a specific ORME according
to this invention is based upon the presence of a doublet in the IR spectrum, the reconstitution of
each ORME back to its constituent T-metal, and its unique performance in specific applications
compared to the constituent T-metal.

ORMEs are transformed into their original T-metal by means of a chemical bonding with an
electron-donating element, such as carbon, which is capable of d orbital electron overlap and
"spin flip". When the G-ORME is chemically bonded to carbon in an aqueous solution of ethyl
alcohol under a specific potential, carbon monoxide is formed and the ORME forms Au+Au+, a
black precipitate, which under continued application of potential and dehydration reduces to
Au+1 Au-1, a metallic bonded diatom of gold. This invention establishes that a high potential
applied to the solution forces an electron into the d orbital, thus eliminating the electron pair. The
first potential, which for G-ORME is approximately -2.2 V and for other ORMEs is between -1.8
and -2.2 V, re-establishes the d orbital overlap. The final potential of -2.5 V overcomes the water
potential to deposit gold onto the cathode.

ORMEs are single T-metal atoms With no d orbital overlap. ORMEs do not conform to rules of
physics which are generally applied to diatoms or larger clusters of metals (e.g., with conduction
bands). The physics of the electron orbitals are actually more similar to those relating to a gas or
solid solution which require density evaluation between atoms at greater distances. Conversely,
atomic orbital calculations of high atomic density metals give results that correspond to valence
charge rearrangement.
When the atomic distances of the elements are increased beyond a critical Coulomb distance, an
energy gap exists between the occupied orbitals and the unoccupied orbitals. The atom,
therefore, is an insulator and not a metal. Physicists when determining the electron band energies
of small atom clusters suggest that the occupation of the bands should be rearranged if the total
energy is to be minimized. The metallic electron orbital arrangement leads to calculations for
energies, which results are inconsistent since the energies of the supposedly occupied states are
higher than the supposedly unoccupied states. If this condition is relaxed and the bands allowed
to repopulate in order to further lower the total energy, both bands will become partially filled.
This repopulation, if performed in the presence of an unlimited source of electrons (reducing
conditions), will provide a total energy condition of the atom which is considerably below or
lower than the atom as it exists in a metallic form. this lower energy is the result of orbital
rearrangement of electrons in the transition element. The resultant form of the element is an
ORME.

SCOPE OF THE INVENTION

The formation and the existence of ORMEs applies to all transition and noble metals of the
Periodic Table and include cobalt, nickel, copper, silver, gold, and the platinum group metals
including platinum, palladium, rhodium, iridium, ruthenium and osmium, which can have
various d and s orbital arrangements, which are referred to as T- metals.

The T-metals, when subjected to conventional wet chemistry will disaggregate through the
various known levels, but not beyond a diatom state. The conventional wet chemistry techniques
if continued to be applied beyond the normally expected disaggregation on level (diatom) in the
presence of water and an alkali metal, e.g., sodium, potassium or lithium, will first form a diatom
and then electron orbitally rearrange to the non- metallic, mono-atomic form of the T-metal, ie.,
an ORME.

An ORME can be reaggregated to the T- metal form using conventional wet chemistry
techniques, by subjecting the ORME to a two- stage electrical potential to "oxidize" the element
to the metallic form.

The ORMEs of this invention exist in nature in an unpure form in various materials, such as
sodic plagioclase or calcidic plagioclase ores. Because of their non- metallic, orbitally rearranged
monoatomic form, ORMEs are not detected in these ores as the corresponding "metals" using
conventional analysis and, accordingly, until the present invention were not detected, isolated or
separated in a pure or substantially pure form. Their presence in the nonmetallic form explains
the inconsistent analysis at times obtained when analyzing ores for metals whereby the
quantitative analysis of elements accounts for less than 100% of the ore by weight.

USES OF ORMEs
ORMEs, which are individual atoms of the T-metals and by virtue of their orbital rearrangement
are able to exist in a stable and virtually pure form, have different chemical and physical
characteristics from their respective T-metal. Their thermal and chemical stability, their
nonmetal-like nature, and their particulate size are characteristics rendering the ORMEs suitable
for manyapplications.

Rhodium and iridium S-ORMEs have been prepared which exhibit superconductivity
characteristics. These S-ORMEs, as described herein, are in a lower energy state as compared to
their respective T-metal, and thus have a lower absolute temperature. The absolute temperature
of an S-ORME system as compared to the absolute temperature of its respective T- metal is
significantly lower, similar to the condition existing when a metal goes through a glass transition.
S-ORMEs, having a very low absolute temperature, are good superconductors. These same
characteristics apply to all ORMEs. Accordingly, a new source of superconductive materials is
made available by this invention. These new materials require substantially less energy removal
to reach the super-conductivity state and, therefore, can be used at higher temperatures than
currently availablesuperconductors.

The ORMEs of this invention can be used for a wide range of purposes due to their unique
electrical, physical, magnetic, and chemical properties. The present disclosure only highlights
superconductivity and catalysis, but much wider potential uses exist, including energy
production.

Preparation of G-ORME
G-ORME was prepared from metallic gold as follows:

50 mg gold (99.99% pure) were dispersed in 200 ml aqua regia to provide clusters of gold atoms.
60 ml concentrated hydrochloric acid were added to the dispersion and the mixture was brought
to boll, and continued boiling until the volume was reduced to approximately 10-15 ml. 60 ml
concentrated HCl were added, and the sample brought to boil and checked for evolution of NOCl
fumes. The process was repeated until no further fumes evolved, thus indicating that the nitric
acid had been removed and the gold had been converted completely to the gold chloride.
The volume of the dispersion was reduced by careful heating until the salt was just dry. "Just
dry" as used herein means that all of the liquid had been boiled off, but the solid residue had not
been "baked" or scorched.
The just dry salts were again dispersed in aqua regia and steps (2) and (3) were repeated. This
treatment provides gold chloride clusters of greater than 11 atoms.
150 ml 6M hydrochloric acid were added to the just dry salts and boiled again to evaporate off
the liquid to just dry salts. This step was repeated four times. This procedure leads to a greater
degree of sub- division to provide smaller clusters of gold chloride. At the end of this procedure
an orangish-red salt of gold chloride is obtained. The salt will analyze as substantially pure
Au2Cl6.
Sodium chloride is added in an amount whereby the sodium is present at a ratio 20 moles sodium
per mole of gold. The solution is then diluted with deionized water to a volume of 400 ml. The
presence of the aqueous sodium chloride provides the salt Na2Au2Cl8. The presence of water is
essential to break apart the diatoms of gold.
The aqueous sodium chloride solution is very gently boiled to a just dry salt, and thereafter the
salts were taken up alternatively in 200 ml deionized water and 300 ml 6M hydrochloric acid
until no further change in color is evidenced. The 6M hydrochloric acid is used in the last
treatment.
After the last treatment with 6M hydrochloric acid, and subsequent boildown, the just dry salt is
diluted with 400 ml deionized water to provide a monoatomic gold salt solution of
NaAuCl2'XH2O. The pH is approximately 1.0.
The pH is adjusted very slowly with dilute sodium hydroxide solution, while constantly stirring,
until the pH of the solution remains constant at 7.0 for a period of more than twelve hours. This
adjustment may take several days. Care must be taken not to exceed pH 7.0 during the
neutralization.
After the pH is stabilized at pH 7.0, the solution is gently boiled down to 10 ml and 10 ml
concentrated nitric acid is added to provide a sodium-gold nitrate. As is apparent, the nitrate is an
oxidizer and removes the chloride. The product obtained should be white crystals. If a black or
brown precipitate forms, this is an indication that there is still Na2Au2Cl8 present. If present, it
is then necessary to restart the process at step (1).
If white crystals are obtained, the solution is boiled to obtain just dry crystals. It is important not
to overheat, i.e., bake.
5 ml concentrated nitric acid are added to the crystals and again boiled to where the solution goes
to just dry. Again it is essential not to overheat or bake. Steps (11) and (12) provide a complete
conversion of the product to a sodium-gold nitrate. No chlorides are present.
10 ml deionized water are added and again boiled to just dry salts. This step is repeated once.
This step eliminates any excess nitric acid which may be present.
Thereafter, the just dry material is diluted to 80 ml with deionized water. The solution will have
a pH of approximately 1.This step causes the nitrate to dissociate to obtain NaAu in water with a
small amount of HNO3 remaining .
The pH is adjusted very slowly with dilute sodium hydroxide to 7.0 + 0.2. This will eliminate all
free acid, leaving only NaAu in water.
The NaAu hydrolyzes with the water and dissociates to form HAu. The product will be a white
precipitate in water. The Au atoms have water at the surface which creates a voluminous cotton-
like product.
The white precipitate is decanted off from any dark grey solids and filtered through a 0.45
micron cellulose nitrate filter paper. Any dark grey solids of sodium auride should be redissolved
and again processed starting at step (1).
The filtered white precipitate on the filter paper is vacuum dried at 120C for two hours. The dry
solid should be light grey in color which is HAuXH2O and is easily removed from the filter
paper.
The monoatomic gold is placed in a porcelain ignition boat and annealed at 300C under an inert
gas to remove hydrogen and to form a very chemically and thermally stable white gold
monomer.
After cooling, the ignited white gold can be cleaned of remaining traces of sodium by digesting
with dilute nitric acid for approximately one hour.
The insoluble white gold is filtered on 0.45 micron paper and vacuum dried at 120C for two
hours. The white powder product obtained from the filtration and drying is pure G-ORME. The
G-ORME made according to this invention will exhibit the special properties described in the
"General Description" of this application, including catalytic activity, special magnetic
properties, resistance to sintering at high temperatures, and resistance to aqua regia and cyanide
attack.

Sources for pure G-ORME

http://zptech.net/ams/david-hudson.html
In the late 1970s, David Radius Hudson was farming in Arizona when he came across strange
materials in the soil of his land. He had no idea what they were, but the mystery of them
fascinated him so much that he spent millions of dollars researching them over the next decade.
In 1989, Mr. Hudson was granted several patents for his research and analysis of these materials.

He originated the term Orbitally Rearranged Monoatomic Elements, ORMEs for short. The
scientific research behind and explanations for what David Hudson discovered are complex. His
patents cover ten transitional elements, including some of the more exotic such as ORME
palladium, ORME iridium, ORME ruthenium and ORME osmium.

ORMEs elements have been found to be present in most living cells. One theory is that the
ORMEs elements inside the body make up or determine some of the properties of the tubulin, or
water, inside the cells of the body. The microtubules hold the water inside each cell. The
microtubules also resonate connections between the body's cells. It is believed that when
ORMEs elements are increased in the body, the connection between the cells is strengthened.

David Hudson believes these elements are the light of life. When these disaggregated atoms are
dried and in a macro state, they look like white powder. They resonate through the body,
bringing it balance and harmony. Zeropoint Technologies also strives to help the mind and body
find an equilibrium through cellular communication. Take a look at the information for gold
powder on this site.

Now is the time for Superhealth, both physically and spiritually, and we have the right tools to
help you accomplish it. Even the realm it encompasses is still relatively unknown in mainstream
consciousness, but its popularity is growing by leaps and bounds. This is the year to give your
body the nutrients it needs to operate at peak performance.

This cutting edge technology is summed up in only a few words: monatomic (or monoatomic)
and diatomic elements. Classical science teaches us that the three phases of matter are gasses,
liquids, and solids (but now there are the newer plasmas, condensates and liquid crystals). Some
solids crystallize into lattice structures we call metals. What classical science does not teach us
(because these are new and extreme cutting edge discoveries) is that there is, in fact, another
phase of matter called "monatomic."

These are also known as ORMES (Orbitally Rearranged Monoatomic Elements) or ORMUS and
m-state elements, and the newest theories in physics as they relate to this area of research assert
that some elements on the periodic chart might be diatomic (two atoms) or small atomic cluster
"condensates," which are known in the scientific community as "Bose-Einstein Condensates."
They are becoming more widely known as "m-state" elements. These elements are widely found,
and our products are a rich and highly concentrated form.

Eric Sutton
Sunday, April 27, 2008 5:19 PM

Hi Erik, I am writing to tell you about how impressed I am with your monatomic gold products.
In june of 2006 I was diagnosed with colorado tick fever which rapidly became viral menengitis
and incephelitis. As is often the case with standard western medicine concerning viral illness,
there was nothing to be done but to ride it out and hope for the best. At my worst point, I am told
that I did not open my eyes or move for 2 days. For months I could not work or exert myself
physically or mentally without side effects such as slurring my speach, severe headaches, and
severe fatigue. I was on anti-nasea medication normally taken by patients to counteract effects
from chemo-therapy medication. I took Zango juice as an antiviral help and rode it out for
months. I gradually improved enough to work again with more minor versions of the symptoms
until I pushed to hard months later and found the symptoms kicking in more severely again. I
immediately took some time off to recover and during this time learned of monatomic gold. I
ordered some aquagold from you after researching it and you pretty thoroughly. I began working
again as I needed to pay bills and prior to recieving the gold and realized I was pushing it a bit. I
would work partial days and often essentially pass out when I finished my day and got home.
The day I got home and found the gold waiting for me, I was ready to spend the rest of the
afternoon and evening laying down and falling in and out of sleep. Instead, I took a couple of
teaspoons of it straight from the bottle, and proceeded to spread a half a dumptruckload of gravel
by hand around my driveway that had been sitting there waiting for me for the last month. My
headache left, my fatigue abruptly improved and continued to gradually do so until it all left. I
have continued to taken the aquagold on a somewhat regular basis ever since and have evaded
every cold and flu or other illness that has run through my house, as well as erasing the fogginess
and mental unclarity that was left by the incephalitis. I have been taking the gold since september
of 2007 and plan to continue to do so indefinitely. Thank you Erik for your research into and
development of these products. Sincerely, Eric Sutton.

Thursday, February 14, 2008 pm MDT

I don't know exactly how to describe "how" it makes me feel better, but it certainly does. And
rapidly, no little blue gel pill is faster, not even close.

After thinking on it a bit more, (a little erudition is not a bad thing) I will put up a n update on the
Migraine Issue page (and change the color!!).

I do the Gold at night (pre-meditation), but have not mixed it with HoloSync as yet.
I will not be advancing in the HoloSync System, but I am certain I will do at least 6 more months
on either Gold or Zynergy. If I can manage, both, as the Zynergy definitely has more fix-it,
within it.
Maybe you are on to something good for migraines with the Indium!!

You know you mentioned timing, and this seems to be a place where things got worse, and the
pain is now constant. So certainly there is healing to be done. The cause of damage seems to be
pressure in this case, not EM as I was fighting back in 2006-7.

After I update Migraine Issues, I will link all the pages to my main page, and I will post The
Observations Pages to the O.R.M.E.s groups I belong to (about 8).

I am convinced.
I really like your products!!
(And the pretty things were very nice too! I don't have to hunt in my foil, paper and bubble wrap
containment area so long & I can do it without looking).

Sally Keiser

----------------------------------------------
Erik,

I just want you to know that I love your Zerolight. I have making and taking ORMUS products
for several years now and by far the Zerolight seems to cover all areas. I just wish I could afford
it all of the time. Thank you Erik!

Don Gifford.

It's truly amazing stuff. Our users are raving about the results they're experiencing. Reports have
indicated huge boosts in mental and physical energy, aches and pains vanishing, increased
mental clarity and focus, increased strength, stamina and sex drive, looking and feeling younger,
and huge boosts in strengthening the immune system.

New Video
Juicing and Monoatomics

http://www.cocoonnutrition.org/catalog/page_monatomic_newsletter.php

MONATOMIC MINERAL NUTRITION, HAVE YOU

EVER HEARD OF IT?
In 1994 I was introduced to a discovery of David Hudson called monatomic minerals. He found
elements existing in a newly discovered state of matter. Minerals in the singular state are able to
interact with the DNA and cause them to relax and recombine corrected. This was proven with
the monatomic form of Iridium.

I have tried around 6 different supposed monatomic mineral supplements over the years and
none of them produced results like David Hudson talked about.

Until now! Recently I was introduced to three products that supply these unique monatomic
minerals in high concentration. The foundation product is called Mineral Magic; it is a one-
pound container with a rare earth powder that has amazing effects in people’s bodies. The
gentlemen that introduced Mineral Magic to me was diabetic at the time and after 8 days on this
rock powder he no longer needed insulin. Within 6 months his grey hair had returned to its full
brown color.

He then went on to develop two other products that are Platinum Group Elixir and White Gold
Liquid. Platinum Group Elixir and White Gold Liquid are pure monatomic elements.

I’ve been on them now for over two weeks. My liver function has improved a lot. I can tell
because I have a better appetite and my eyes are no longer puffy a sign of liver congestion. My
eyes look the best they’ve looked in 10 or more years. I’m sleeping the best I’ve slept in 10
years. My mind is clearer and I even feel like I’m floating inside my head sometimes since being
on these minerals. The Gold has a pronounced effect on my brain and perceptions in a very
positive way. I can see solutions to my own problems much easier and move on from them. This
is truly and physical, mental and spiritual food. I’m amazed. I will be considering these as the
most important supplement to take from this point forward.

Additionally, Andrea is having equally amazing results. For the first time in 10 years her hair has
stopped falling out. Usually she loses 5 to 6 handfuls of hair a day. Yesterday she lost only two
hairs. For the first time in 10 years she has gone to the Chiropractor and her back is holding the
adjustments. Her memory is coming back. She has outstanding energy. The enamel on her teeth
feels stronger. She also looks much younger and she wakes up without bags or dark circles under
her eyes. She also has had profound mental emotional insights and experiences of a spiritual
nature. She feels very happy.

Mineral deficiencies are at the foundation of all degenerative disease. These minerals will begin
to rewrite your life in a very positive way.

To the awakening of your heart and mind,

Stephen Heuer,

Nutripath and Overseer of Cocoon Nutrition

=====================================================================

http://www.cocoonnutrition.org/catalog/page_ormus.php
Chinese tradition holds that sickness, pain, and other health problems are caused when Chi
energy is blocked. When Chi flows freely, Chi energy heals and restores the body. ORMUS
concentrate products helps to remove energy blockages and create vital energy balance.

WHAT IS IT?

ORME or ORMUS has only recently been recognized as a fourth state of matter over and above
solid, liquid and gas.

WHAT WILL IT DO?

Think of each of the cells of your body as a tired drained battery that can be recharged and
rejuvenated by the elemental life force released by ORMUS Concentrate Products

HEALING and REJUVENATION

Many have made claims for healing and rejuvenation but we believe that those abilities are
inherent in the strong healthy body and positive attitude which the naturally balanced minerals in
ORMUS Concentrate Products can help to achieve.

MENTAL ENHANCEMENT

Others attest to enhanced mental clarity, calmness, increased intuitive powers, insightfulness and
a sense of connection to a higher state of awareness

A man named David Hudson has done much pioneering research over the last two decades and
has been granted numerous patents for the Orbitally Rearranged Monatomic Elements or ORME.

These products are called VULCAN'S TREASURE and HERMES' ELIXIR, but throughout
history they have been called many things: Chi, prana, soma, manna, ORME, Ormus, M-State,
white powder gold, the Eye of Horus, the Elixir of Life, the Holy Grail, sorcerers stone, and the
Philosopher's Stone of alchemy.

In the past, when the concentrate has been available, it was only for the highest members of the
ruling class and priesthood. It is our goal to make high quality ORMUS concentrate products
available to all who become aware of its virtue.

It is recommended to approach Ormus Liquid Concentrates on a gradient scale. Vulcan's

Treasure should be used first, followed by Hermes' Elixir. When the products are used as
recommended, the effects may be profound.

VULCAN'S TREASURE - ORMUS MONO ATOMIC

CONCENTRATE
Vulcan's Treasure is the first level in the ingestible Ormus Concentrate. The source material for
this extract comes from the Forge of the Gods, a living volcano. This mineral extract is made
from the highly paramagnetic volcanic ejecta of Mount St. Helens. In the past, only a very few
were able to partake of this type of M-State extract, as it was too unstable to be shipped without
losing its essence. The source material is gathered in the shadow of the volcano to produce the
first stable extract of this kind. The volcanic extract is blended with Liquid Chi to produce a very
potent product which is named, Vulcan's Treasure. For maximum effect, Ormus Concentrates
should be approached on a gradient. Vulcan's Treasure will remove blockages and balance
energy, making way for Hermes' Elixir to proceed similarly on other levels. These changes
cannot be rushed and must proceed at their own pace for maximum benefit.
Read the Vulcans Treasure Assay here.

HERMES' ELIXIR - ORMUS MONO ATOMIC

CONCENTRATE
This is a unique ORMUS concentrate product. Never before has a product of this kind been
offered to the public. It is made by taking Liquid Chi and dehydrating it by 80%. To this super-
concentrate is added alchemical "Wine of Gold" and it is then reconstituted to the original
volume. This gives a final product which is both full strength Vulcan's Treasure and 80% "Wine
of Gold". A scientific study done by Belmar pharmacy has shown that colloidal gold has been
proven to raise IQ scores in as little as 30 days. The spiritual effects of Hermes' Elixir are unique.

Read the Hermes Elixir Assay here.

Cocoon Nutrition now recommends ISO 77, the latest advance in monatomic element technology
- click here to learn more

http://www.subtleenergies.com/ORMUS/tw/sciover.htm

ORMUS - Scientific Overview

by Barry Carter
I am working with a group of scientists and laypersons that are exploring the properties of a
group of elements that appear to exist in a new state of matter. These elements in this state
exhibit a number of Bosonic properties at biological temperatures and have been measured in
various biological systems.(1)

We have determined that these are the precious metal elements in a non-metallic state, which we
call ORMUS or m-state. We have also determined that these m-state elements are much more
abundant in nature than their metallic counterparts.

We have extracted the m-state elements from water, air and rock. We believe that many of the
familiar properties of water are the result of the presence of the ORMUS elements in it.(2)

We believe that the m-state elements were not previously isolated and identified because they
exist as Cooper-paired Bosons without available valence electrons and which, therefore, are not
susceptible to spectroscopic identification.(3)

While there are a number of simple methods to concentrate, extract or convert these materials it
is still quite difficult to make positive identification of the elements involved.(4) Positive
identification requires that the m-state element be converted to its metallic counterpart and then
identified using spectroscopy.

Since these elements have been isolated from brain tissue at a fairly high level, (5% by dry
matter weight) we believe that they may play a crucial role in consciousness. Perhaps as a
quantum-coherent, superconducting system in the microtubules of the cell.(5)

At this point we are still very low on the learning curve in relation to the ORMUS elements. We
can isolate and identify them. We can convert metal to m-state and m-state to metal. Some of us
have been ingesting these materials for several years in a more concentrated form. A few
biological studies have been done and more are planned. We have demonstrated effects, which
suggest superconductivity at biological temperatures.(6) People with a variety of illnesses have
ingested these materials with amazing results.(7) Some technological uses have been explored
but nothing is to a marketable point. And, several good ORMUS products have become available
for purchase.(8)

We have not quantified or replicated many of our observations. Many of our theories are based
on one or two observations and need to be further verified.

These materials look like they may be the keystone in the bridge between science and spirit.

I have set up a number of email forums for discussion of, and research into, the ORMUS
materials and their implications. Let me know if you are interested in learning more about the m-
state elements and I can direct you to the proper venue.

http://www.subtleenergies.com/ormus/faq.htm

ORMUS FAQ by Barry Carter

Questions
• How can I get some of the monoatomic White Powder Gold?
• What is the difference between ORMUS, m-state and ORME?
• Will the "good stuff", the real White Powder Gold, allow me to
ascend?
• Which product is best for me?
• Why does ORMUS "dislike" magnetic fields?
• Does anyone sell ORMUS materials?
• What has happened to David Hudson?
• How can I get in touch with others who are interested in ORMUS?
• How can I learn more about ORMUS?
• Are there any reports from people who have used these materials?
• How might I contribute to ORMUS research?
• Has anyone ever noticed any ill effects after ingesting ORMUS
materials?
• Are there any books out on this subject?
 • How do I contact the author of this site?

Question: How can I get some of the monoatomic White Powder Gold?

Answer: It has not been conclusively demonstrated whether the strange

materials David Hudson identified are monatomic or not. Some scientists have
suggested that the only way they could have the properties that they have is if
they are di-atomic or greater.

Since we do not wish to prejudice the scientific process we have decided not
to call them monatomic unless this issue is resolved. Instead we call them m-
state or ORMUS elements. The “m” in m-state could mean monatomic,
microcluster or even manna. You can read a scientist’s explanation of why
these elements should not be monatomic at:

paranorm.htm#diatomic

Apparently, David Hudson used the term "White Powder Gold" as a generic
term for all of the precious metal elements in their m-state form. Hudson never
made very much of the white powder of gold because his ore source had
relatively little m-gold in it.

David Hudson's colleague who did the 41 day fast was using a powder
composed of several m-state elements with less than 1% of the powder being
white gold. The current thinking of most experts, including Hudson, is that
once the m-state is dried out into a powder it is much less easy for the body to
assimilate.

It is possible to purchase m-state gold in a relatively pure form as a wet

precipitate. Many of the people who have tried the m-state gold for a length of
time do not like it for a variety of reasons. Some feel that it makes them
lethargic. Some feel that it puts them so much in the moment that they forget
to do the things which are important to make their lives work. One long-term
researcher claims that the m-gold "locks" a person into their present condition,
whatever that may be.

The easiest way to get m-state gold is to use the Wet Method on Dead Sea
salt as the resulting precipitate is claimed to be 70% m-gold and 30%
magnesium.

You can see what percentage of the m-state elements is in various seawater
sources at:
ormus4.htm

Your best way to get the m-state materials is to make them yourself using the
methods described at:

ormus2.htm

Question: What is the difference between ORMUS, m-state and ORME?

Answer: The three terms above all mean pretty much the same thing but they
originated in different situations.
I learned how to make the white precipitate from the Essene on May 18, 1997.
He called all of the white precipitates from various sources m-state. These
sources included the white precipitate from the Wet Method on ocean water or
Dead Sea salt and the white precipitate from the Sodium Burn on metallic gold
and black sand. He also referred to David Hudson's products as m-state and,
when I told him of the ORMUS products that Jim made from metal using
ozone we both spoke of these substances as being m-state materials.

Just prior to my first visit with the Essene we set up a "private" email list to
evaluate and promote various ORMUS production methods. The folks on this
list (about 60 people) agreed to the following wording of the ORMUS method
document after nearly a year of experimentation and discussion:

"Since Hudson has patented his process for obtaining and identifying
these elements, we would like to suggest that the terms ORMUS and m-
state be used when referring to this state of matter."

It was our intention to honor Hudson by using his term "ORMUS" and to honor
the Essene by using his term "M-State". Both of these terms were originally
used to cover all of these elements as they occur in a non-metallic form in
nature.

We rejected the use of the acronym ORME (which stands for Orbitally Re-
arranged Monoatomic Element) because there was no good scientific
evidence that these materials were orbitally re-arranged or monatomic. I still
have not seen any evidence of this.

You can read a longer explanation of the reasons for these definitions at:

definitions.htm

You can read a discussion about why many of us do not think they are
monatomic at:

what.htm
Question: Will the "good stuff", the real White Powder Gold, allow me to
ascend?

Answer: People are always asking about the ability of the white powder of
gold to act as a sort of "enlightenment pill". An "enlightenment pill" would be
some substance that would cause any person who takes it to instantly
transcend, ascend, awaken or "see" God.

Belief in the concept of an enlightenment pill seems to be rooted in the deeper

belief that enlightenment can come from outside of the self. This belief is
almost the same as the belief that someone else is responsible for the mess
that "I" am in right now.

Let's imagine that the ORMUS elements can improve the connection to spirit.
Now, let's pretend that each of us is actually responsible for everything which
has ever happened to us. Imagine that you are responsible for the
manifestation of what you want and also responsible for the manifestation of
what you don't want, in your life.

If the ORMUS elements are a connecting medium between "spirit and

mind/matter" then they might work sort of like the air which connects us with
the resonance of sound. I can speak and, if the air is thick enough to sustain
life, you can hear what I say.

If the air is thicker, like at sea level, the sound of my voice will travel faster and
clearer than if the air is thinner, like on a mountain top. This is the reason that
you can hear a train coming, by putting your ear to the iron rail, long before
you can hear the train through the air. The denser the substance the faster
sound will travel through it. ORMUS would be a very dense medium for
carrying our thoughts and feelings.

Now imagine that you are standing on a ledge in the Grand Canyon. You
shout out a word and a few seconds later the echo comes back to you. It
startles you because it seems like someone else is standing next to you and
has shouted back the same thing that you shouted. Perhaps you shouted out
"I love you" or perhaps you shouted out "I hate you".

The Grand Canyon is so big that the echo is delayed a long time. This makes
it seem that the echo you hear is coming from someone else. If you hear the
words "I love you" you feel really good about yourself but if you hear the
words "I hate you" you might become frightened because you think that
someone wishes to harm you.
If the ORMUS elements are a medium of communication between mind and
spirit they would bring us back the echo of whatever we are thinking about
ourselves.

Suppose you had two bells outside your front door. One of these bells sounds
wonderful and the other sounds horrible. The wonderful sounding bell attracts
laughing, happy children to your front door and the horrible sounding bell
attracts violent, vicious criminals to your door.

Now suppose that the wonderful bell rings whenever you think about what you
want and the horrible bell rings whenever you think about what you don't want.
What would happen if the air, which carries the sound of the bell, suddenly
became thicker. What if it became infinitely thick so that every thought would
instantly manifest those things that were in resonant harmony with it.

I think that this is what happens with ORMUS, especially the "good stuff". I
think it carries the resonance of our thoughts and beliefs and brings back the
echo of their manifestation very quickly. If this is true then here is a way to tell
if you are ready for the "good stuff".

First, examine your life--do things you don't like ever happen to you? Would
you be happier if these things were intensified and more instantly connected
to the thoughts that called them in? Conversely, notice how regularly the
things you do like happen to you. When you wake up in the morning do you
contemplate your day with delicious anticipation or do you dread going to
work? Which bell do you ring as you go out your front door?

Your beliefs are habits, which ORMUS will not change. When you take
ORMUS it does not steal your free choice. It does not make you think only of
what you want and prevent you from thinking of what you don't want. You still
can choose which bell you are going to ring with each thought. Are you sure
you always think of your angels and never think of your demons--for
whichever you think of you will manifest in your life and this manifestation will
only be hastened and heightened by the ingestion of the "good stuff".

You can read a cautionary story about the "good stuff" at:

realthing.htm

Question: Which product is best for me?

Answer: You are changing all of the time. The best product for you today
might not be the best one for you tomorrow or next year. Each of us is
different. There is no single product which is best for all people. Some
products may be better for certain conditions than others but, at this point, we
do not know which product is best for which condition.
Your best bet for finding a product which works well for you is to try several
different products. Have someone muscle test you on each of them. Read the
WhiteGold list and archives for the effects that others have reported for the
product of interest.

Question: Why does ORMUS "dislike" magnetic fields?

Answer: In his Tampa workshop David Hudson said:

1:47:35 - I've found that there are four substances that pin these high spin atoms and
take them back to the low spin state. Those substances are sulfites (SO3), carbon and
carbon monoxide, nitric oxide, and short wavelength radiation (deep ultraviolet or
shorter). That's what caused this stuff to explode in sunlight, I found out later. So
there are four major things which cause this to go back to the low spin state. So,
actually, in your body there are four things which cause this to go back to the low spin
state. So that in your body it kills the light. It causes them to go back to the low spin
state.

1:48:15 - I will say that when nitric oxide interreacts with these elements,
taking them back to the low spin state, that it does involve a phenomenon
called electron annihilation. And the actual nitric oxides instead of being
nitrogen 14 becomes radioactive carbon 14 when that occurs. So that in your
body, when dying you are producing radioactive carbon 14. It gets in your
body a different way than they tell you it does.

When Jim learned this he realized that his ozone was probably doing something
similar and that is why he had the fibers of gold grow inside his hands.

Based on these experiences Jim designed the first magnetic traps to get ORMUS to
levitate out of ordinary ground water. The traps work on the principle that the
ORMUS in the water is repelled by the magnetic fields in the trap. Jim also did
another experiment in which he pulsed a very high energy magnetic field under
concentrated ORMUS liquid. This liquid "boiled like gasoline" though it was not
warm at all. We postulate that the gas coming off of the liquid was ORMUS vapor.

From these and other experiences we hypothesized that the Meissner effect on the
ORMUS causes it to retreat from electromagnetic fields. We believe that this effect is
energizing for the ORMUS at first but that when it reaches a certain level (Hc2) the
Meissner effect breaks down and the superconductive ORMUS drops toward a
metallic state. Don Nance demonstrated this by drying sea water precipitate on an
electric burner, or by exposing it to UV light, or by microwaving it in a microwave
oven. In each case, there was an increase in the metallic content of the precipitate
which further increased over a period of six months.
Based on all of this, we have concluded that ORMUS is energized at first when
exposed to high energy electromagnetic fields but is later moved toward the metallic
state as the field exposure continues. Since we don't have any way to identify the
break over point, we recommend that you avoid exposing ORMUS to sunlight or
electromagnetic fields.

This would include things like cordless phones, cell phones, bluetooth devices,
microwave ovens, electric burners, wireless networks and high voltage electric lines. I
also try to avoid hanging out in line with the axis of spin of motors, hard drives and
electric generators.

<>Question: Does anyone sell ORMUS materials?

Answer: If, for some reason, you cannot make your own there are several
good sources for these materials. These sources are listed in no particular
order since I do not wish to suggest a preference. In fact, there are many
people who prefer each of these sources and I suspect that each will meet the
needs of different people. ORMUS Sources

Question: The most recent information on the Internet about David Hudson
and his production facility is dated 1996. What has happened since then with
David Hudson and his plans?

Answer: Mr. Hudson is not in production. There is some question about

whether he will ever get into production.

David Hudson has faced a number of difficulties in getting his ORMUS

production on line. When his plant was five days into a test run in the summer
of 1998, a nitric acid tank sprang a leak. Fortunately Hudson had a concrete
catch basin, which contained the acid. Unfortunately the emergency response
team from the fire department sprayed foam on the acid instead of simply
diluting it with water. The foam reacted with the acid and generated a large
cloud of orange nitric acid gas. Several hundred people had to be evacuated
from the surrounding area.

As a consequence of this event Hudson was fined and forced to think about
moving his plant.

A short time after the acid leak Hudson had a heart attack. He had to have six
bypasses. Subsequent to his surgery he had additional heart problems but
seems to be doing well now.

His plant is still not ready for production. The delays cost him a great deal of
money and this set him back even further. Now he must move his plant into a
properly zoned area. In November of 2000 he sent out his last newsletter titled
"ENOUGH IS ENOUGH" in this newsletter he suggested that his plant has
been "regulated out of existence".

His most recent public lecture was a December 99 lecture in Dallas which was
videotaped by the Eclectic Viewpoint.

Question: How can I get in touch with other people who share my interest in
the ORMUS materials?

Answer: There are several email lists for discussion of ORMUS and related
topics.

I recently set up a new forum for newcomers to the ORMUS field of study.
This forum is on YahooGroups and is called simply ORMUS. Here are the
commands for this list:

Post message: ORMUS@yahoogroups.com

Subscribe: ORMUS-subscribe@yahoogroups.com
Unsubscribe: ORMUS-unsubscribe@yahoogroups.com
List owner: ORMUS-owner@yahoogroups.com

You can also subscribe on line at:

http://groups.yahoo.com/group/ORMUS/

When you subscribe to this list you will be sent a message requesting more
information about you and how you learned about this list. You must send a
response to this request in order before I will add you to the list. This is
necessary to prevent spammers from joining the list and posting.
The main ORMUS forum is called the WhiteGold List. The WhiteGold List is a
moderated email list. This means that the moderator of the list reviews every
post you send to the list before it gets sent on to the whole list.

Since its inception in February of 1996 it has been the policy of the WhiteGold
List to keep the names and contact information of its subscribers as private as
those subscribers wish to be. We determine whether a person wishes to make
this kind of information available to the entire list by whether or not they
include this kind of information in the body of their post or in their signature
lines. If you include only your first name at the bottom of your post that is all
that will be included in the "From:" line in the header.

The WhiteGold List is for the sharing of personal experiences with the
ORMUS substances. There is some scientific discussion but we discourage
religious and political discussion because of the great diversity of people who
are interested in ORMUS. The WhiteGold List averages about 25 messages
per day. To join the WhiteGold list send a message to WhiteGold-
request@zz.com with the subject Subscribe.

The WhiteGold list is a very active list. Folks on the list are generally quite
willing to answer questions so you may generate some interesting responses
by posting your questions to this list.

If you do not wish to get 25 or more emails a day from the WhiteGold list, you
have the option of joining the digest version of the list. All of the posts are
there but you get them in one digest message a day. To join the WhiteGold
digest list send a message to WhiteGold-request@zz.com with the subject
Subscribe digest.

If this does not work contact sumro@zz.com .

The ORMUS and Spirit list was created as a place where people can freely
discuss religious and spiritual issues. Anyone can join this list and it is not
moderated or anonymous. This forum averages about one message per day.
Here are the commands for this list:

Post message: ORMUSandSpirit@yahoogroups.com

Subscribe: ORMUSandSpirit-subscribe@yahoogroups.com
Unsubscribe: ORMUSandSpirit-unsubscribe@yahoogroups.com
List owner: ORMUSandSpirit-owner@yahoogroups.com

You can also subscribe on line at:

http://groups.yahoo.com/group/ORMUSandSpirit/

When you subscribe to this list you will be sent a message requesting more
information about you and how you learned about this list. You must send a
response to this request in order before I will add you to the list. This is
necessary to prevent spammers from joining the list and posting.

In addition to these forums there are over 100 local area ORMUS email lists.
There is generally a local list centered within a hundred miles of most places
in the United States and there are over 25 lists outside the USA.

These local ORMUS lists were created so that people can meet in person to
work together on ORMUS related stuff. I also post information about
upcoming ORMUS related meetings and lectures when they are to occur in a
local area.

Contact me for a link to these local ORMUS email lists.

They are not moderated or anonymous. If you would like to set up a

workgroup in your area please let me know what country you live in and what
city you live near. I regularly get reports of results from people, on these local
lists, who have been making and ingesting their own m-state materials.

I initially started setting up the local area ORMUS email lists in January of
1999 so that folks who are interested in ORMUS would have a way to get
together in person to work on ORMUS related projects. Some of the projects
that I envisioned at the time are:

• Learning to make ORMUS using a variety of methods.

• Sharing resources to make ORMUS cooperatively.
• Sharing the costs of trying numerous ORMUS products (ORMUS
"tasting" parties).
• Purchasing ORMUS related supplies in bulk.
• Building magnetic traps.
• Cooperative ocean expeditions to collect ocean water.
• Comparing personal ORMUS experiences.
• Setting up presentations for local and non-local speakers.
• Swapping ORMUS related books and videos.
• Organizing strategies to better get the word out about ORMUS.

While all of these joint projects are useful in themselves they also help to build
community among people who have many common goals and values. I
believe that community building is a very important thing right now. People
who are good at working together are most likely to prosper in times of
changing social structures.

I would like to encourage everyone who reads this to join a local ORMUS
group. I am looking for volunteers to coordinate the local groups.

Remember, it is always best to have your own local source of supply for
something as precious and useful as ORMUS.

Question: How can I learn more about ORMUS?

Answer: You can find basic descriptions of ORMUS at:

ORMUS – Basic Overview by Barry Carter

ORMUS – What is it?

ORMUS - Scientific Overview by Barry Carter

An illustrated article on ORMUS can be found at:

Ancient Puzzles

by Barry Carter

Articles on various ORMUS related subjects can be found at:

Articles.htm

David Hudson's lectures, patents and other related materials can be found at:

What Is It?

Question: Are there any reports from people who have used these materials?

Answer: You can find a number of these reports at:

reports.htm

Question: How might I contribute to ORMUS research?

Answer: There are many ways you can contribute. Two ways that I would
suggest initially are to support this work financially by donating money and
contribute by documenting your ORMUS experiences.

If you wish to make a monetary contribution contact me at sumro@zz.com.

Everyone who uses ORMUS is in a great position to contribute to our

understanding of what it is and how it works. The easiest way to do this is to
document the changes you experience with it.

Some of the most remarkable documentation that we have is from those few
people who thought to take before pictures of problem areas. I just wish more
people would do this.

One of the best set of pictures we have is the before and after picture of the
tooth at:

tooth.jpg

and the beard at:

m-copperbeard.jpg

The "after" picture alone totally looses its impact without the "before" picture
for comparison.

I just wish we had the before picture for Tut's tail at:
tutstail.htm

I also wish I had a before picture of the hands described in this quote:

"My hands were claw-like, arched and impossible to lay flat, with all fingers
splayed apart due to the calcium deposits on the knuckles that forced the
fingers outward. Each joint has calcium deposits that have twisted the fingers;
in addition to looking old and awful, very painful. I can now lay my hands flat,
and the fingers on the right hand are almost completely touching each other."

We have an after picture at:

hands.jpg

In this case one picture would have been worth much more than 67 words.

I asked this woman to take a before picture but she put it off. She did not
expect the changes to happen so quickly.

Here is a list of documentation steps which would help the cause if lots of
folks were to start them before starting their use of the ORMUS substances.

1. List all of your existing health problems and get a medical checkup which
will document the existence of these problems.

2. Photograph every part of the body that might change with ORMUS
ingestion. The following areas are particularly suggested:

a. The face including details of wrinkles and sagging skin.

b. Hair color. Get good close ups of any hair which has become gray.

c. Hair growth patterns and thickness (this would include baldness and hair
loss)

d. Both sides of both hands.

e. Any scars, skin cancers or skin conditions like psoriasis or shingles.

 f. Swollen joints like finger joints, knees, wrists and elbows.

g. Any broken or cracked teeth and visible cavities.

g. A good picture of the spine which might show any spinal misalignment.

h. A picture which shows the whole body profile.

I. A picture which shows the whole body from the front.

j. A picture which shows the whole body from behind.

The last three pictures would reveal hip rotations, differences in leg or arm
lengths or other posture problems and should be taken with little or no clothing
on. If you are modest about this sort of thing you can take the pictures with a
film camera, leave the film undeveloped and store it in a safe place. Women
may wish to take photos which show breast size and sag as both conditions
have been known to change with the use of ORMUS substances.

These pictures can be taken with a digital camera, a disposable film camera,
a video camera or a regular film camera. Every person will not need to take
every picture. Just take pictures of those areas where change might happen.

3. Make tracings of the feet and hands. Some people have reported that their
fingers and toes have gotten longer.

4. Measure your height. This should be done immediately after rising from bed
in the morning as this is the time of maximum height during the day. Some
people may get as much as 1.5 inches shorter over the course of the day.
Several people have reported ORMUS related changes in their height. One
woman has gotten 3.5 inches taller at the age of 53.

5. Check the pH of your saliva and urine first thing in the morning and last
thing at night for a week before starting with a new ORMUS product.

6. Document changes in frequency, color, odor and ease of urination.

7. Document any changes in stool softness, regularity, color and whether it

floats or not.

8. Document any changes in the sound you hear when things are quiet. Many
people have reported that they hear a sound in their head after using ORMUS
for a while. This sound is called the "hu" or "nada". Notice any changes in the
frequency of this sound, it's intensity or the nature of the sound. I always hear
a high frequency sound at around 11,000 Hz and occasionally hear a chirping
sound in my right ear. You can download a trial version of the NCH Tone
Generator which can be used to compare frequency at:

http://www.nch.com.au/tonegen/

9. Document any noticeable changes in tooth pain, new teeth, tooth

alignment, filling in of cavities or other changes in the teeth.

10. Women should document any changes in their period including changes in
the level of menstrual cramping, PMS, periodicity changes, flow levels and
resumption of menstruation after menopause.

11. Everyone should document changes in sexual response or orgasm

intensity.

12. Some people have noticed that it is easier to quit addictive behaviors like
smoking or other drug use. If you have any such addictions it would be helpful
to document how those addictions change with the use of ORMUS.

13. Hair analysis can reveal mineral deficiencies over time. Before and after
hair analysis would be helpful.

14. Blood tests can reveal immune system changes and/or cancer indicators.
If you think that these things might be changing with your ORMUS ingestion it
will be helpful to get copies of these tests from your doctor.

15. If anyone can think of any other things to add to this list I will make the
changes.

If you are interested in helping out with ORMUS research but not quite
interested enough to do all of the things listed above, documenting any portion
of the list will be much better than doing nothing at all. This list order is a
rough approximation of the order of importance of these various
documentation tasks.

Question: Has anyone ever noticed any ill effects after ingesting ORMUS
materials?

Answer: Occasionally people have reported unpleasant effects associated

with the use of some of the ORMUS products listed on the SubtleEnergies
web site. Most of these effects might be explained as follows:

First, the ORMUS elements appear to stimulate the body's elimination of

toxins. This occurs first at the cellular level. As these toxins re-enter the blood
stream they can trigger the same symptoms that they triggered when the
toxins were originally stored in the cells. These symptoms generally do not
persist as long as they did originally but they may be a bit more intense for a
short period of time. They are also reported to happen in reverse order from
the present to the past. This process is called a "healing crisis". You can read
a diary which describes these healing crisis effects from trap water at:

Trap Water Diary

The liver and kidneys have the role of cleansing toxins from the blood and
eliminating them from the body. If these organs are not functioning well there
can be a buildup of toxins in these organs which might harm them. For this
reason it is generally best to do a series of liver cleanses and drink lots of
water in conjunction with the initial stages of ORMUS ingestion. From my
experience, few people have serious problems with this cleansing stage.

For some people the increased elimination load might result in constipation.
The extra magnesium in ocean water ORMUS precipitate can mitigate this as
it is the same as the active ingredient of milk of magnesia a notable laxative.
An extra benefit is that most people are magnesium deficient and this is a
good magnesium source.

Concurrent with the elimination process some people report tiredness or

sleepiness. The Essene reported that during this stage some folks will get
quite sleepy and that when they wake up they will "eat everything but the
curtain rods and then they will go right back to sleep again." We think that this
happens because the body is using up the energy stored in ATP to fuel the
healing process. There are some indications that this tiredness can be
prevented or mitigated by taking extra B vitamins, especially B-12 and the
amino acid creatine.

Another issue that has been suggested by several ORMUS researchers and
producers is that it is easier to benefit from ORMUS if the body is in a more
alkaline state. There is some evidence that ORMUS products, particularly
those with a magnesium or calcium base, will tend to alkalize the body. Other
ORMUS sources appear to work better when the body is slightly alkaline.
Most people on the conventional American diet tend to be acidic. The
following foods and situations tend to move one toward the alkaline end of the
spectrum:

All vegetables especially green leafy vegetables

Most all fruits including citrus fruits

Millet, Quinoa

Drink several glasses of spring water daily

Ripe olives

Raw almonds

Lima beans, Soy beans

Fresh green peas & green beans

Avocado

Goat milk (Contains lactose)

Low protein/low fat diet

Whey (contains milk sugar, lactose)

Ghee (clarified butter, a cholesterol-free saturated fat)

Moderate exercise

Relaxation exercises, i.e. deep breathing, yoga, etc.

The following foods and situations tend to move one more toward the less
desirable acid end of the spectrum:

Excessive consumption of starches

All seafood. fish fowl ! & all flesh foods

Yogurt, butter, eggs. cow's milk, cheese

Wheat, oats. barley, rice, corn, bread, spelt

Kamut, amaranth, teff, buckwheat

All beans except lima and soy beans

High fat meals (more than 20% of calories from fat)

High protein diet (over 25 grams per day)

All pastas, macaroni, and noodles.

Crackers, chips
Overeating

Cooked tomatoes, pasta & sauce

Refined Sugar, corn syrup. honey, soda pop

Cookies, cakes, pies, sweets, etc.

Blueberries, cranberries, currants, plums, prunes

Carob

Allergic reactions

All nuts & seeds (except almonds)

Tobacco, Drugs

Margarine, lard, hydrogenated oils, corn & olive oil

All fried foods (fried in ghee. butter or oils)

Coffee, tea, alcohol, chocolate

Low water intake

Over exercise, lack of sleep

Anxiety, anger, worry, stress

Experts in this arena suggest that one should consume about 80% alkaline
forming foods and 20% acid forming foods. You can find a chart with more
information on this subject at:
balance.htm

Finally, David Hudson and others have suggested that certain substances can
"pin" the ORMUS elements to their metallic state under some circumstances.
These conditions apparently can happen in the body. According to Hudson
the substances in question are sulfites (SO3), carbon and carbon monoxide
and nitric oxide. Since most of the ORMUS elements are toxic in their metallic
form it is wise to avoid foods and situations which increase these substances
in the body. There are some indications that the tendency for the ORMUS
elements to drop to metal is minimized by having an adequate B-12 intake.

Question: Are there any books out on this subject?

Answer: You can find an ORMUS related booklist at:

booklist.htm

=====================================================================

You can find more information on the items referenced in the text at the following links:

(1) Natural Sources of ORMUS Materials

http://www.subtleenergies.com/ormus/health/sources.htm

(2) Living Water, Vital Air

http://www.subtleenergies.com/ormus/tw/livwater.htm

Promising New Technologies

http://www.innerx.net/personal/tsmith/newtech2.html

Homeopathic Resonances and ORMUS

http://www.subtleenergies.com/ormus/tw/homeopat.htm

(3) Manipulating the ORMUS elements

http://www.subtleenergies.com/ormus/tw/Manipula.htm

(4) Methods
http://www.subtleenergies.com/ormus/tw/methods.htm

(5) ORMUS and Consciousness

http://members.aol.com/yggdras/paraphysics/BCarter.htm

(6) Magnetic Levitation "Movie"

http://www.subtleenergies.com/ormus/research/levitate.avi

(7) Health Effects of the ORMUS Elements

http://www.subtleenergies.com/ormus/health/health.htm

(8) ORMUS FAQ

http://www.subtleenergies.com/ormus/faq.htm

I have written a number of other articles, which also might be of interest:

Patterns of Motion
http://www.subtleenergies.com/ormus/tw/patterns.htm

Paramagnetic Forest Soils

http://www.subtleenergies.com/ormus/tw/paramag.htm

ORMUS and Quantum Evolution

http://www.subtleenergies.com/ormus/tw/evolution.htm

ORMUS Variations
http://www.subtleenergies.com/ormus/tw/variation.htm
ORMUS, DNA Repair and Health
http://www.subtleenergies.com/ormus/tw/dna.htm

http://www.rexresearch.com/ormes/ormes.htm REX RESEARCH on Hudson.

http://www.rexresearch.com/ormes/hudsnlec.htm REX RESEARCH “Has the Philosopher’s

Stone Been Found?”

http://www.lyghtforce.com/WhiteGold/ White Gold Mail List & David Hudson Information.

YOUTUBE Related Videos

http://www.youtube.com/watch?v=68jtnuMAa00 Philosopher’s Stone, Make your own.
http://www.youtube.com/watch?v=ifFggud9ppQ&feature=related How to make ORMES Gold
http://www.youtube.com/watch?v=NDAtlmyJzbA&feature=related Ormus Warning construction
tips.
http://www.youtube.com/watch?v=Hg_4pUmGIU8&feature=related How to make an Ormus
Shaker.
http://www.youtube.com/watch?v=9n7Qpk9wAqs&feature=related How to make an Ormus
water bubbler.